US3268332A - Electrophotographic element - Google Patents

Electrophotographic element Download PDF

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Publication number
US3268332A
US3268332A US197596A US19759662A US3268332A US 3268332 A US3268332 A US 3268332A US 197596 A US197596 A US 197596A US 19759662 A US19759662 A US 19759662A US 3268332 A US3268332 A US 3268332A
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United States
Prior art keywords
binder
styrene
percent
copolymer
weight
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Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Expired - Lifetime
Application number
US197596A
Inventor
Paul J Caruso
Richard P Flynn
Gerald L Mcleod
David S Most
Herbert N Schlein
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Northrop Grumman Guidance and Electronics Co Inc
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Itek Corp
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Priority to US197596A priority Critical patent/US3268332A/en
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Publication of US3268332A publication Critical patent/US3268332A/en
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    • GPHYSICS
    • G03PHOTOGRAPHY; CINEMATOGRAPHY; ANALOGOUS TECHNIQUES USING WAVES OTHER THAN OPTICAL WAVES; ELECTROGRAPHY; HOLOGRAPHY
    • G03GELECTROGRAPHY; ELECTROPHOTOGRAPHY; MAGNETOGRAPHY
    • G03G5/00Recording members for original recording by exposure, e.g. to light, to heat, to electrons; Manufacture thereof; Selection of materials therefor
    • G03G5/02Charge-receiving layers
    • G03G5/04Photoconductive layers; Charge-generation layers or charge-transporting layers; Additives therefor; Binders therefor
    • G03G5/05Organic bonding materials; Methods for coating a substrate with a photoconductive layer; Inert supplements for use in photoconductive layers
    • G03G5/0528Macromolecular bonding materials
    • G03G5/0532Macromolecular bonding materials obtained by reactions only involving carbon-to-carbon unsatured bonds
    • G03G5/0535Polyolefins; Polystyrenes; Waxes
    • GPHYSICS
    • G03PHOTOGRAPHY; CINEMATOGRAPHY; ANALOGOUS TECHNIQUES USING WAVES OTHER THAN OPTICAL WAVES; ELECTROGRAPHY; HOLOGRAPHY
    • G03GELECTROGRAPHY; ELECTROPHOTOGRAPHY; MAGNETOGRAPHY
    • G03G5/00Recording members for original recording by exposure, e.g. to light, to heat, to electrons; Manufacture thereof; Selection of materials therefor
    • G03G5/02Charge-receiving layers
    • G03G5/04Photoconductive layers; Charge-generation layers or charge-transporting layers; Additives therefor; Binders therefor
    • G03G5/05Organic bonding materials; Methods for coating a substrate with a photoconductive layer; Inert supplements for use in photoconductive layers
    • G03G5/0528Macromolecular bonding materials
    • G03G5/0532Macromolecular bonding materials obtained by reactions only involving carbon-to-carbon unsatured bonds
    • G03G5/0539Halogenated polymers
    • GPHYSICS
    • G03PHOTOGRAPHY; CINEMATOGRAPHY; ANALOGOUS TECHNIQUES USING WAVES OTHER THAN OPTICAL WAVES; ELECTROGRAPHY; HOLOGRAPHY
    • G03GELECTROGRAPHY; ELECTROPHOTOGRAPHY; MAGNETOGRAPHY
    • G03G5/00Recording members for original recording by exposure, e.g. to light, to heat, to electrons; Manufacture thereof; Selection of materials therefor
    • G03G5/02Charge-receiving layers
    • G03G5/04Photoconductive layers; Charge-generation layers or charge-transporting layers; Additives therefor; Binders therefor
    • G03G5/05Organic bonding materials; Methods for coating a substrate with a photoconductive layer; Inert supplements for use in photoconductive layers
    • G03G5/0528Macromolecular bonding materials
    • G03G5/0532Macromolecular bonding materials obtained by reactions only involving carbon-to-carbon unsatured bonds
    • G03G5/0546Polymers comprising at least one carboxyl radical, e.g. polyacrylic acid, polycrotonic acid, polymaleic acid; Derivatives thereof, e.g. their esters, salts, anhydrides, nitriles, amides
    • GPHYSICS
    • G03PHOTOGRAPHY; CINEMATOGRAPHY; ANALOGOUS TECHNIQUES USING WAVES OTHER THAN OPTICAL WAVES; ELECTROGRAPHY; HOLOGRAPHY
    • G03GELECTROGRAPHY; ELECTROPHOTOGRAPHY; MAGNETOGRAPHY
    • G03G5/00Recording members for original recording by exposure, e.g. to light, to heat, to electrons; Manufacture thereof; Selection of materials therefor
    • G03G5/02Charge-receiving layers
    • G03G5/04Photoconductive layers; Charge-generation layers or charge-transporting layers; Additives therefor; Binders therefor
    • G03G5/05Organic bonding materials; Methods for coating a substrate with a photoconductive layer; Inert supplements for use in photoconductive layers
    • G03G5/0528Macromolecular bonding materials
    • G03G5/0557Macromolecular bonding materials obtained otherwise than by reactions only involving carbon-to-carbon unsatured bonds
    • G03G5/056Polyesters
    • YGENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y10TECHNICAL SUBJECTS COVERED BY FORMER USPC
    • Y10STECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y10S525/00Synthetic resins or natural rubbers -- part of the class 520 series
    • Y10S525/904Activation of preformed polymer in absence or monomer, for subsequent polymerization thereon, e.g. trapped radicals

Description

United States Patent M 3,268,332 ELECTROPHOTOGRAPHIC ELEMENT Paul J. Caruso, West Newton, Richard P. Flynn, Somerville, Gerald L. McLeod, Lexington, David S. Most, Peabody, and Herbert N. Schlein, Framingham, Mass., assignors to Itek Corporation, Lexington, Mass., a corporation of Delaware No Drawing. Filed May 25, 1962, Ser. No. 197,596
2 Claims. (Cl. 96-1) This invention relates to cohesive media, and relates in particular to cohesive binder matrices for solid particles, and to articles incorporating such binder matrices.
The present invention concerns new cohesive and adhesive binder matrix materials for finely divided solid particles. Although the materials of the invention are useful as matrix materials in a wide variety of useful applications, and for the embodiment of numerous different kinds of particulate solids, they are of special utility as binders for coating image forming media, particularly those used in electrostatic or persistent internal polarization reproducing processes.
Image reproduction techniques involving electrostatic processes, such as those discussed in the RCA Review (1959), pages 753-769, or persistent internal polarization phenomena, such as those discussed in Physical Review, volume 97, No. 6 (1955), pages 1596-1610, are conveniently practiced with image forming media comprising a substrate coated with finely divided particles of a photoconductor or phosphors applied to the substrate in a binder matrix. The substrate, Which preferably is flexible, may be porous or non-porous, such as of paper, wood, cloth, glass or metal. The binder is an insulating material in which the semiconductor or phosphor particles are embedded, and which adheres the particles to the substrate.
The present invention relates to new binder compositions superior to those known in the art for preparing image forming media in being highly flexible, having an unusually high capacity for solids, being strongly adhesive to substrate materials coated therewith, having good rhe ological properties permitting easy handling during mixing and coating, and giving humidity impervious coatings with excellent insulating properties which impart to the finished media a slow dark decay and a capacity for accepting a large electrostatic charge (in electrostatic proc esses, for example). The last mentioned properties are of particular utility for giving images of high contrast and low background. In addition, the new binder systems are compatible with certain particularly convenient nonfiammable volatile liquid developers. Liquid developers, which comprise finely divided particles dispersed in a liquid, are commonly used to develop latent electrostatic and polarization images.
The new binder matrices of the invention comprise three resinous components. The first component is a high resistivity styrene-containing material. Although poly styrene has a desirable high resistivity, it is a relatively inflexible material, and copolymers of styrene containing at least about 10-15% of a rubbery diolefinic comonomer such as butadiene, isoprene or chloroprene are preferred for use in the invention. Additionally, ternary copolymers of styrene, a rubbery component and acrylonitrile have excellent abrasion resistance and improved dielectric constant, as compared with the binary copolymers just mentioned. In such ternary materials, the acrylonitrile may be present in amounts up to about by weight of the polymer.
The second resinous component of the new binders is a flexible, adhesive polyvinylidene chloride polymer or copolymer having a high solids capacity. Particularly suitable materials are various grades of Saran, i.e. polyvinylidene chloride homopolymers or copolymers con- 3,268,332 Patented August 23, 1966 taining up to 10-15% acrylonitrile. These resins are excellent mechanical binders for solids and impart capacity for holding solids, without loss of adhesive properties, to the compositions of the invention.
The third resinous component in the binders is a high resistivity material contributing flexibilty and plasticity to the binder, and acting principally to reduce foam in the solvent-binder-solid systems employed in coating substrate materials. The foam-reducing components are alkyd resins, suitably soya-based alkyd resins such as those produced by reacting phthalic acid with soya bean alcohols.
In the binders of the invention, the three resinous components are preferably present such that a major portion of the binder by Weight comprises the styrene-containing copolymer, at least a major portion of the balance is a polyvinylidene chloride polymer or copolymer, and the balance is the alkyd defoaming resin. In general, the binder should contain at least 50% of the styrene-containing component, at least 25% of the polyvinylidene chloride component, and at least /2% of the alkyd defoaming resin. Particularly preferred binders are obtained when these three components are in a preferred weight ratio of 4:2:1.
For admixture with finely divided solids and application to a suitable substrate, the resins of the invention are combined in a mutual solvent. Although other solvents dissolving all three of the resins can be employed, ketone materials have proved especially desirable as solvents, and the binders are conveniently obtained by dispersing the resinous components in an aliphatic ketone such as acetone, methyl ethyl ketone, dibutyl ketone, or cyclic aliphatic ketones such as cyclohexanone.
The resin solutions are then combined with the solid materials to be dispersed in a binder. Although the solids can be dispersed in the solution in amounts such that on drying the resulting coatings will contain only about 10 percent by weight of binder, particularly good results are obtained when the solids to binder ratio by Weight does not exceed about 7:1 (about 14 percent of binder). Of course, lower ratios of solids to binder can be employed, but it is generally desirable to have as high a solids to binder ratio as is compatible with good results.
The resulting dispersions of solids in dissolved resin binders are conventionally applied with a doctor blade, roll coaters, spot coaters, curtain coaters, or the like, in an amount of about 8-25 pounds/ 3000 ft. on a dry solids basis (binder plus pigment). Particularly good image reproducing media are obtained with a coating of about 15-25 pounds of dry solids per 3000 ft. of backing. After application, the coatings are dried, either by simple air drying or by forced drying using heat.
A better understanding of the invention and of its many advantages will be had by referring to the following example, given by way of illustration.
Example 1 122.5 parts by weight of finely divided zinc oxide, 10 parts by weight (based on dry solids content) of a highimpact styrene-butadiene copolymer, 5 parts by weight of polyvinylidene chloride polymer, and 2.5 parts by weight of soya-based alkyd resin were dispersed in sufficient methyl ethyl ketone (about 200 parts by weight) in agitated mixing means for about one minute to form a slurry.
The slurry was then conventionally applied as a coating to a conductive paper backing in a thickness of about 15- 25 pounds per 3000 ft. The coating was then baked for 3 minutes at C.
The resulting paper is useful for electrostatic reproducing processes wherein, for example, the surface of the coated paper is uniformly electrostatically charged by a corona discharge device. The charged surface is then selectively discharged by exposure to a light image. Where light strikes the charged paper, rendering the zinc oxide particles photoconducting, the charge is dissipated. The latent electrostatic image remaining on the paper can be developed by sprinkling the paper with finely divided opaque particles, such as of carbon black, having a charge opposite to that of the image.
As known in the art, the photosensitivity of semiconductor materials such as zinc oxide can be increased in the visible region by sensitizing the particles with suitable dyes. Thus, a particularly desirable paper for electrostatic printing purposes is prepared when the zinc oxide of the sample comprises three equal portions of zinc oxide, each respectively sensitized with Auramine, Alpha Azurine, and Rose Bengal. Other suitable photoconductive semiconducting materials are oxides such as titanium dioxide and the like.
Paper suitable for use in persistent internal polarization reproduction processes can be prepared in a similar fashion by substituting photoconductive insulating materials exhibiting persistent internal polarization for the zinc oxide materials of the example. Suitable materials are phosphors such as numerous doped zinc sulfides, cadmium sulfide, and mixed (ZnzCd) S phosphors.
Development of the media prepared with the binders of the present invention is preferably performed using a liquid developer comprising nonflammable volatile liquids which are poor solvents for the binder substance, i.e. liquids which swell and tackify but do not dissolve the binder. Finely divided opaque particles, such as of carbon black, are suitable suspended in these fluids with the use of a substance imparting an electric charge, usually a positive charge to the suspended particles.
For use with the binders of the present invention, developers containing a chlorinated or chlorofluorinated aliphatic hydrocarbon having two to four carbon atoms and a boiling point above about 40 C. as the suspending liquid have proved particularly advantageous. These materials include certain relatively involatile liquids known under the trade names Freon, Ucon, and Genetron. If desired, these liquids may be combined with chlorinated solvents such as methylene chloride, carbon tetrachloride, chloroform, perchloroethylene, and the like, to decrease the solvent action of the fluorine-containing materials on the binders.
As opaque particles for suspension in these fluids, carbon black has proved particularly advantageous. As a charge imparting substance, mixed hydrocarbon substances commercially available as lubricants under the trade name of Coblax are particularly suitable, as disclosed in copending U.S. patent application Serial No. 123,03 8.
A liquid developer particularly suitable for use with the resin binders disclosed herein comprises Freon T (CCIF CFCI having a boiling point of about 50 C.,
in optional admixture with up to 520% by volume of carbon tetrachloride and containing about 4-8 grams per liter of a mixture containing one part by weight of carbon black and from 36 parts by weight of a charge-imparting substance such as the commercial material Coblax, which is a mixture of asphaltic polycyclic hydrocarbons, largely aromatic, but having long straight chain aliphatic residues attached thereto, and having a molecular weight of about 1500.
Although specific embodiments have been shown and described herein, it Will be understood that they are but illustrative.
What is claimed is:
1. In a radiation responsive image forming medium comprising a substrate having thereon a photoconductive insulating coating comprising photoconductive particles in an electrically insulating binder matrix therefor, the improvement in which said binder comprises, in combination, (A) at least about 50 percent by Weight of a member of the group consisting of a homopolymer of styrene, a binary copolymer of styrene and a diolefinic comonomer, and a ternary copolymer of styrene, a diolefinic comonomer, and acrylonitrile, (B) at least about 25 percent of a member of the group consisting of a homopolymer of vinylidene chloride and a copolymer of vinylidene chloride with acrylonitrile, and (C) at least /2 percent of an alkyd resin.
2. A radiation responsive image forming medium as in claim 1 wherein component (A) is a ternary copolymer of styrene containing at least about 1015 percent of said diolefinic cornonomer and up to about 25 percent by weight of acrylonitrile, and component (B) is a copolymer of vinyliclene chloride and up to 10-15 percent of acrylonitrile.
References Cited by the Examiner UNITED STATES PATENTS 2,786,785 3/1957 Wise 260-454 2,877,203 3/1959 Forsythe et a1. 260-454 2,919,206 12/ 1959 Malmquist 260-454 2,986,521 5/1961 Wielicki 252-621, 3,011,999 12/1961 Parker et al. 260-454 3,051,569 8/1962 Sugarman et al 96-1 3,066,023 11/1962 Schlesinger 96-1 3,079,342 2/1963 Insalaco 252-621 3,088,927 5/ 11963 Dissen 260-454 3,121,006 2/1964 Middleton et a1 96-1 3,121,008 2/1964 Jones et a1. 96-1 3,128,179 4/1964 Kendall et al. 96-1 NORMAN G. TORCHIN, Primary Examiner.
T. J. HOFFMAN, Assistant Examiner.

Claims (1)

1. IN A RADIATION RESPONSIVE IMGE FORMING MEDIUM COMPRISING A SUBSTRATE HAVING THEREON A PHOTOCONDUCTIVE INSULTING COATING COMPRISING PHOTOCONDUCTIVE PARTICLES IN AN ELECTRICALLY INSULATING BINDER MATRIX THEREFOR, THE IMPROVEMENT IN WHICH SAID BINDER COMPRISES, IN COMBINATION, (A) AT LEAST ABOUT 50 PERCENT BU WEIGHT OF A MEMBER OF THE GROUP CONSISTING OF A HOMOPOLYMER OF STYRENE A BINARY COPOLYMER OF STYRENE AND A DIOLEFINIC COMONOMER, AND A TERNARY COPOLYMER OF STYRENE, A DIOLEFINIC COMONOMER, AND ACRYLONITRILE, (B) AT LEAST ABOUT 25 PERCENT OF A MEMBER OF THE GROUP CONSISTING OF A HOMOPOLYMER OF VINYLIDENE CHLORIDE AND A COPOLYMER OF VINYLIDENE CHLORIDE WITH ACRYLONITRILE, AND (C) AT LEAST 1/2 PERCENT OF AN ALKYD RESIN.
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Cited By (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3378370A (en) * 1964-02-06 1968-04-16 Interchem Corp Recording elements for electrostatic printing
US3907693A (en) * 1973-05-21 1975-09-23 Rank Xerox Ltd Liquid developer for electrophotography
US3963486A (en) * 1973-05-21 1976-06-15 Rank Xerox Ltd. Electrophotographic imaging process employing epoxy-ester containing liquid developer
JPS5212837A (en) * 1975-07-19 1977-01-31 Konishiroku Photo Ind Co Ltd Electrophotographic light sensitive composition
US4581311A (en) * 1981-08-06 1986-04-08 Fuji Photo Film Co., Ltd. Photoconductive composition with vinylidene chloride-acrylonitrile copolymer additive
US5322755A (en) * 1993-01-25 1994-06-21 Xerox Corporation Imaging members with mixed binders

Citations (12)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2786785A (en) * 1955-03-28 1957-03-26 Dow Chemical Co Coating for rubber mats
US2877203A (en) * 1955-06-29 1959-03-10 Armstrong Cork Co Polyvinyl halide composition containing oxidized polyester resin, and method of making same
US2919206A (en) * 1957-03-21 1959-12-29 Du Pont Coated book cover material
US2986521A (en) * 1958-03-28 1961-05-30 Rca Corp Reversal type electroscopic developer powder
US3011999A (en) * 1958-10-30 1961-12-05 Armstrong Cork Co Vinyl resin composition containing 1, 3-butylene isophthalate as a plasticizer
US3051569A (en) * 1959-10-26 1962-08-28 American Photocopy Equip Co Photoconductive materials
US3066023A (en) * 1958-12-19 1962-11-27 Azoplate Corp Member for electrophotographic reproduction and process therefor
US3079342A (en) * 1960-02-12 1963-02-26 Xerox Corp Electrostatic developer composition and method therefor
US3088927A (en) * 1959-09-10 1963-05-07 Velsicol Chemical Corp Oil modified alkyl resins modified with a thermal polymer of dicyclopentadiene
US3121008A (en) * 1959-04-09 1964-02-11 Eastman Kodak Co Photoconductive zinc oxide compositions comprising oxonol, hemioxonol, or benzylidene dyes
US3121006A (en) * 1957-06-26 1964-02-11 Xerox Corp Photo-active member for xerography
US3128179A (en) * 1960-09-02 1964-04-07 Eastman Kodak Co Cyanine dye-sensitized photoconductive compositions comprising zinc oxide

Patent Citations (12)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2786785A (en) * 1955-03-28 1957-03-26 Dow Chemical Co Coating for rubber mats
US2877203A (en) * 1955-06-29 1959-03-10 Armstrong Cork Co Polyvinyl halide composition containing oxidized polyester resin, and method of making same
US2919206A (en) * 1957-03-21 1959-12-29 Du Pont Coated book cover material
US3121006A (en) * 1957-06-26 1964-02-11 Xerox Corp Photo-active member for xerography
US2986521A (en) * 1958-03-28 1961-05-30 Rca Corp Reversal type electroscopic developer powder
US3011999A (en) * 1958-10-30 1961-12-05 Armstrong Cork Co Vinyl resin composition containing 1, 3-butylene isophthalate as a plasticizer
US3066023A (en) * 1958-12-19 1962-11-27 Azoplate Corp Member for electrophotographic reproduction and process therefor
US3121008A (en) * 1959-04-09 1964-02-11 Eastman Kodak Co Photoconductive zinc oxide compositions comprising oxonol, hemioxonol, or benzylidene dyes
US3088927A (en) * 1959-09-10 1963-05-07 Velsicol Chemical Corp Oil modified alkyl resins modified with a thermal polymer of dicyclopentadiene
US3051569A (en) * 1959-10-26 1962-08-28 American Photocopy Equip Co Photoconductive materials
US3079342A (en) * 1960-02-12 1963-02-26 Xerox Corp Electrostatic developer composition and method therefor
US3128179A (en) * 1960-09-02 1964-04-07 Eastman Kodak Co Cyanine dye-sensitized photoconductive compositions comprising zinc oxide

Cited By (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3378370A (en) * 1964-02-06 1968-04-16 Interchem Corp Recording elements for electrostatic printing
US3907693A (en) * 1973-05-21 1975-09-23 Rank Xerox Ltd Liquid developer for electrophotography
US3963486A (en) * 1973-05-21 1976-06-15 Rank Xerox Ltd. Electrophotographic imaging process employing epoxy-ester containing liquid developer
JPS5212837A (en) * 1975-07-19 1977-01-31 Konishiroku Photo Ind Co Ltd Electrophotographic light sensitive composition
JPS5613307B2 (en) * 1975-07-19 1981-03-27
US4581311A (en) * 1981-08-06 1986-04-08 Fuji Photo Film Co., Ltd. Photoconductive composition with vinylidene chloride-acrylonitrile copolymer additive
US5322755A (en) * 1993-01-25 1994-06-21 Xerox Corporation Imaging members with mixed binders

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